Evidence map›Paper›PMID 40084363›Full record

ArticleAmerican journal of cancer research2025

Dissecting the high-risk property of 1q gain/amplification in patients with newly diagnosed multiple myeloma.

Xinyue Liang, Weiling Xu, Fan Zhou, Wenyang Huang, Xingcheng Yi, Yingjie Zhang, Yurong Yan, Nan Zhang, Jingxuan Wang, Xiaoxiao Sun and 9 more

Abstract read
In one paragraph

Article in American journal of cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Xinyue LiangDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Weiling XuDepartment of Radiology, The First Hospital of Jilin University Changchun, Jilin, China.
Fan ZhouDepartment of Hematology and Oncology, Shanghai Jing'an District Zhabei Central Hospital Shanghai, China.
Wenyang HuangState Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Science and Peking Union Medical College Tianjin, China.
Xingcheng YiLaboratory of Cancer Precision Medicine, The First Hospital of Jilin University Changchun, Jilin, China.
Yingjie ZhangDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Yurong YanDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Nan ZhangDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Jingxuan WangDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Xiaoxiao SunDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Rui HuDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Yufeng ZhuDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Xintian MaDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.
Yue SunLaboratory of Cancer Precision Medicine, The First Hospital of Jilin University Changchun, Jilin, China.
Maozhou LanLaboratory of Cancer Precision Medicine, The First Hospital of Jilin University Changchun, Jilin, China.
Mengtuan LongLaboratory of Cancer Precision Medicine, The First Hospital of Jilin University Changchun, Jilin, China.
Shaji K KumarDivision of Hematology, Mayo Clinic College of Medicine Rochester, MN, USA.
Yun DaiLaboratory of Cancer Precision Medicine, The First Hospital of Jilin University Changchun, Jilin, China.
Fengyan JinDepartment of Hematology, The First Hospital of Jilin University Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1q gain/amplification (1q+) is the most common cytogenetic abnormality (CA), with a frequency of 30-50% in patients with newly diagnosed multiple myeloma (NDMM). Although accumulating evidence supports 1q+ as a "high-risk" CA (HRCA), several issues remain to be addressed to understand its true prognostic property. We retrospectively analyzed a cohort of 934 patients with NDMM from three centers in China, who had baseline data available for 1q+ [including 1q21 gain (3 copies) and amplification (> 3 copies)] detected by fluorescence in situ hybridization in isolated CD138

Indexed as

1q gaincytogenetic abnormalitydouble hitminimal residue diseasemultiple myeloma

Identifiers

PMID40084363
PMCPMC11897644

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.